Make your mark in global health by managing high-impact clinical trials with a leading CRO.

Hobson Prior is seeking a Clinical Research Coordinator to join a clinical research site in Skierniewice, Poland, on a part-time freelancing basis. This role involves supporting clinical studies by managing data, coordinating study visits, and ensuring compliance with study protocols. The position is for 20 hours per week over a 6-month contract, with an ideal start date as soon as possible.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

• Prepare for study visits and ensure all necessary materials are ready.
• Enter data into systems and resolve any queries related to the data.
• Schedule and remind participants of their appointments.
• Verify data accuracy and upload source documents.
• Monitor adverse events (AE) and serious adverse events (SAE).
• Ensure compliance with electronic diary (e-diary) requirements.

Key Skills and Requirements:

• Experience in a similar role, such as a Study Coordinator or Clinical Research Coordinator.
• Strong organizational skills to manage schedules and data entry tasks.
• Attention to detail for verifying and monitoring study data.
• Ability to work independently and communicate effectively with team members.

For more information, please contact Terrah-Leigh Pietersen.

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.

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